Yolk sac macrophage progenitors traffic to the embryo during defined stages of development

Christopher Stremmel(LMU Klinikum), R. Schuchert(LMU Klinikum), Franziska Wagner(LMU Klinikum), Raffael Thaler(LMU Klinikum), Tobias Weinberger(LMU Klinikum), Robert Pick(Ludwig-Maximilians-Universität München), Elvira Mass(Memorial Sloan Kettering Cancer Center), Hellen Ishikawa‐Ankerhold(LMU Klinikum), Andreas Margraf(Ludwig-Maximilians-Universität München), Sonja Hutter(Klinik für Frauenheilkunde), Ronald J. Vagnozzi(Cincinnati Children's Hospital Medical Center), Sarah Klapproth(Max Planck Institute of Biochemistry), Jon Frampton(University of Birmingham), Simon Yona(Weizmann Institute of Science), Christoph Scheiermann(Ludwig-Maximilians-Universität München), Jeffery D. Molkentin(Cincinnati Children's Hospital Medical Center), Udo Jeschke(Klinik für Frauenheilkunde), Markus Moser(Max Planck Institute of Biochemistry), Markus Sperandio(Ludwig-Maximilians-Universität München), Steffen Maßberg(LMU Klinikum), Frédéric Geissmann(Memorial Sloan Kettering Cancer Center), Christian Schulz(LMU Klinikum)
Nature Communications
January 2, 2018
Cited by 285Open Access
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Abstract

Abstract Tissue macrophages in many adult organs originate from yolk sac (YS) progenitors, which invade the developing embryo and persist by means of local self-renewal. However, the route and characteristics of YS macrophage trafficking during embryogenesis are incompletely understood. Here we show the early migration dynamics of YS-derived macrophage progenitors in vivo using fate mapping and intravital microscopy. From embryonic day 8.5 (E8.5) CX 3 CR1+ pre-macrophages are present in the mouse YS where they rapidly proliferate and gain access to the bloodstream to migrate towards the embryo. Trafficking of pre-macrophages and their progenitors from the YS to tissues peaks around E10.5, dramatically decreases towards E12.5 and is no longer evident from E14.5 onwards. Thus, YS progenitors use the vascular system during a restricted time window of embryogenesis to invade the growing fetus. These findings close an important gap in our understanding of the development of the innate immune system.


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